Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 2:9605728 (forward strand)|View in location tab

Co-located variant

dbSNP rs540959701 (T/-)

Most severe consequence
 
Intron variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 36 sample genotypes.

Variant displays